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Structure of 374564-34-8
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Potassium (3-bromophenyl)trifluoroborate delivers a trifluoroborate handle for palladium-catalyzed cross-coupling reactions. This bench-stable reagent integrates readily into synthetic sequences, offering high functional group tolerance and efficient transformation under mild conditions.
Potassium (3-bromophenyl)trifluoroborate serves as a stable, bench-ready boron source for Suzuki-Miyaura cross-coupling reactions. Its trifluoroborate group enables efficient palladium-catalyzed aryl-aryl bond formation with broad functional group tolerance. The reagent exhibits excellent stability under ambient conditions and facilitates straightforward purification, making it ideal for iterative synthesis of complex biaryls and pharmaceutical scaffolds.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: